Variant report

Variant	rs566418820
Chromosome Location	chr22:32492990-32492991
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	22:31836635-31847259..22:32487779-32494662	K562	blood:
2	22:32487779-32494662..22:33339333-33353583	GM12878	blood:
3	22:32487779-32494662..22:32860159-32865649	GM12878	blood:
4	22:32012966-32043914..22:32487779-32494662	K562	blood:
5	22:32170492-32188129..22:32487779-32494662	K562	blood:
6	22:32487779-32494662..22:33452523-33459358	K562	blood:
7	22:32487779-32494662..22:32594665-32606395	K562	blood:
8	22:32487779-32494662..22:32764253-32784733	GM12878	blood:
9	22:32487779-32494662..22:32878464-32886640	GM12878	blood:
10	22:32487779-32494662..22:32872511-32874561	K562	blood:
11	22:32487779-32494662..22:32740683-32750950	K562	blood:
12	22:32228866-32235273..22:32487779-32494662	K562	blood:
13	22:32487779-32494662..22:32920308-32927723	K562	blood:
14	22:32487779-32494662..22:32750950-32761732	GM12878	blood:
15	22:32487779-32494662..22:33190123-33206921	GM12878	blood:
16	22:32053085-32061138..22:32487779-32494662	K562	blood:
17	22:31914965-31930706..22:32487779-32494662	K562	blood:

No data

Variant related genes	Relation type
ENSG00000271093	Chromatin interaction
ENSG00000233733	Chromatin interaction
ENSG00000205853	Chromatin interaction
ENSG00000184708	Chromatin interaction
ENSG00000100150	Chromatin interaction
ENSG00000198089	Chromatin interaction
ENSG00000184459	Chromatin interaction
ENSG00000100225	Chromatin interaction
ENSG00000232218	Chromatin interaction
ENSG00000252909	Chromatin interaction
ENSG00000128253	Chromatin interaction
ENSG00000185666	Chromatin interaction
ENSG00000241878	Chromatin interaction
ENSG00000254127	Chromatin interaction
ENSG00000128276	Chromatin interaction
ENSG00000241954	Chromatin interaction
ENSG00000230736	Chromatin interaction
ENSG00000242082	Chromatin interaction
ENSG00000243519	Chromatin interaction
ENSG00000100234	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1060529	chr22:32370432-32525699	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv834177	chr22:32416679-32594663	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	esv1803811	chr22:32441022-32509431	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv948789	chr22:32462505-32764760	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1065175	chr22:32467617-32761093	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
6	nsv544680	chr22:32467617-32761093	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
7	esv2830423	chr22:32477718-32767825	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
8	esv2422247	chr22:32486448-32788258	Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv834178	chr22:32490449-32677521	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
10	nsv3596	chr22:32491329-32507091	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32473400-32495000	Weak transcription	Colonic Mucosa	Colon
2	chr22:32473600-32495600	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr22:32476200-32495800	Weak transcription	Stomach Mucosa	stomach
4	chr22:32476600-32499400	Weak transcription	Pancreas	Pancrea
5	chr22:32485600-32498400	Weak transcription	Small Intestine	intestine
6	chr22:32486400-32508400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr22:32490200-32504000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr22:32491200-32511400	Strong transcription	Duodenum Mucosa	Duodenum
9	chr22:32491400-32493600	Strong transcription	Fetal Intestine Large	intestine
10	chr22:32491800-32493400	Strong transcription	Fetal Intestine Small	intestine
11	chr22:32492000-32493000	Genic enhancers	Fetal Heart	heart
12	chr22:32492000-32493200	Enhancers	Right Ventricle	heart
13	chr22:32492200-32493400	Enhancers	Left Ventricle	heart

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